Plumbridge J A, Dondon J, Nakamura Y, Grunberg-Manago M
Nucleic Acids Res. 1985 May 10;13(9):3371-88. doi: 10.1093/nar/13.9.3371.
Protein and operon fusions between lacZ and various genes of the nusA,infB operon have been constructed on lambda bacteriophages and used to show that the operon is negatively regulated by the level of NusA protein. Overproducing NusA (but not IF2) from a multicopy plasmid reduces the level of beta-galactosidase from the fusions indicating repression of the operon. Introducing the lambda carrying the fusions into nusA mutant strains produces a higher level of beta-galactosidase-indicative of derepression of the operon. In particular, a larger form of the NusA protein which does not affect bacterial growth per se causes a derepression of the operon. As both protein and operon fusions respond equivalently, we conclude that the nusA protein is acting at the transcriptional level to regulate expression of the nusA, infB operon.
已在λ噬菌体上构建了lacZ与nusA、infB操纵子各基因之间的蛋白质和操纵子融合体,并用于表明该操纵子受NusA蛋白水平的负调控。从多拷贝质粒过量表达NusA(而非IF2)会降低融合体中β-半乳糖苷酶的水平,表明操纵子受到抑制。将携带融合体的λ噬菌体导入nusA突变菌株会产生更高水平的β-半乳糖苷酶,这表明操纵子去抑制。特别是,一种本身不影响细菌生长的更大形式的NusA蛋白会导致操纵子去抑制。由于蛋白质融合体和操纵子融合体的反应相同,我们得出结论,nusA蛋白在转录水平上起作用,以调节nusA、infB操纵子的表达。